FDA Drug Recalls

Recalls / Firms / Teva North America

Teva North America

12 FDA drug recalls on record.

DateClassDrugStatus
2016-08-05Class IIIClaravis (isotretinoin capsules USP), 10mg, packaged in carton containing 3 Blister PacksTerminated
2016-07-15Class IIIChildren's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Terminated
2016-06-24Class IIAmoxicillinTerminated
2016-06-22Class IIAlbuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by ConTerminated
2016-06-17Class IILinezolid Injection 600 mg/300 mL Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALTerminated
2016-06-17Class IIEptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial, For Intravenous Use OnlyTerminated
2016-06-17Class IIARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, ManufacturTerminated
2016-06-17Class IIOndansetron Injection USP 40 mg/20 mL (2 mg/mL), Rx Only, Manufactured in Hungary for TEVATerminated
2016-05-31Class IIImitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial Terminated
2016-05-18Class IIIDivalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, ManufacturedTerminated
2016-04-27Class IILinezolid Injection, 600 mg/300 mL Single use container bags (NDC 0703-9060-31), packaged Terminated
2015-12-21Class IICapecitabineTerminated